Rate of disintegration is defined as the time required by a sample or substance at which half of the radioactive substance disintegrates. It depends on the nature of disintegration and amount of substance.
The age of the sample is approximately 4241.17 years.
Given that:
C-14 atoms disintegration rates = 15.3 atom/ min-g
Rate of disintegration of the sample = 9.16 atom/ min-g
The digit proportion of carbon-14 is = = 0.5987
Now, also the half-life of carbon-14 is 5730 years.
Such that:
Taking log:
n log 2 = -log 0.5987
Thus, n =
n = 0.740
The age of the sample can be given by:
Age = n x half-life
Age = 0.740 x 5730
Age = 4241.17 years.
Therefore, the age of the substance is 4241.17 years.
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Answer:
The answer is "4,241 .17 years"
Explanation:
The disintegration rate, which shows in C-14 atoms =
Rate of sample disintegration =
The digit proportion of C-14 can be determined that is included in the sample
5730 years from half-life.
The number with half-lives (n) which are repelled must be determined:
So, the age of the sample is given by =
Answer:
is formed of cation, and anion,
Explanation:
Naming of the ionic compounds:-
Hence, given ionic compound:-
is formed of cation, and anion,
Thus, the name must be Cobalt(II) nitrate.
Answer:
To obtain the pH of 8.0, the concentration of NaOCl needs to be 0.9 M in the 0.3 M HOCl solution
Explanation:
This problem can be solved by Henderson-Hasselbalch equation, which gives relation between the concentration of acid, its salt, pKa and the pH of the solution. This equation is given as,
By placing the known variables in the above equation we get,
The above calculations show that the required concentration of NaOCl is 0.9 M.
Speed of the car =
Given time = 37.0 s
Converting time from seconds to hours:
1 hr= 60 min; 1 min = 60 s
Calculating distance from speed and time:
Converting distance from km to m:
So the distance traveled by the car in 37.0 s is 894 m.
Answer:
p orbitals only
Explanation:
Carbon has an atomic number of 6 so its electron configuration will be 1s² 2s² 2p². It has two orbitals as indicated with the 2 as its period number with the outer orbital have 4 valence electrons. So carbon is in the p-orbital, period 2 and in group 4.
Carbon's valence electrons reside in the 2s and 2p orbitals. These orbitals hybridize during bond formation to create equivalent sp3 hybrid orbitals, as evidenced in the methane molecule. Carbon's valence electrons are not placed in d orbitals.
Carbon (atomic number 6) has a total of six electrons. Two of these fill the 1s orbital. The next two fill the 2s orbital, and the final two are in the 2p subshell. According to Hund's rule, the most stable configuration for an atom is one with the maximum number of unpaired electrons. Therefore, carbon has two electrons in the 2s subshell and two unpaired electrons in two separate 2p orbitals. When discussing valence electrons, the electrons in the outermost shell are the ones considered, which for carbon are the electrons in the second shell namely 2s and 2p.
The geometry of the methane molecule (CH4) illustrates that in the bonding process, the s and p orbitals hybridize to allow the formation of four equivalent bonds with hydrogen atoms. Without hybridization, we would expect three bonds at right angles (from the p orbitals) and one at a different angle (from the s orbital). Nonetheless, through orbital hybridization, all four bonds in methane are identical, which is explained by the concept of sp3 hybridized orbitals.
Therefore, the valence electrons for carbon would be placed in the s orbital and p orbitals, not in the d orbitals, because carbon does not have electrons in the d subshell in its ground state. Additionally, the s and p orbitals are the only ones involved in bonding for carbon in most of its compounds, such as methane.
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Answer:
Explanation:
The missing incomplete resonance structure is attached in the image below. From there, we can see the addition of the nonbonding electrons and its' formal charge which makes the resonance structure a complete resonance structure. The others two resonance structure that can be derived from the complete structure is also shown in the image. Out of these three structures, the structure that contributes most to the hybrid is the structure with the negative charge on the oxygen.
To complete the provided resonance structure, add nonbonding electrons and formal charges. Then, draw the two remaining resonance structures by distributing the nonbonding electrons and formal charges differently.
When completing the provided incomplete structure of the anion, you need to add nonbonding electrons and formal charges to make it accurate. Then, draw the two remaining resonance structures by distributing the nonbonding electrons and formal charges differently. To illustrate, let's consider the example of a nitrate ion (NO3-). The complete structure of the provided resonance form would have a double bond between the central nitrogen atom and one of the oxygen atoms, with two lone pairs on the nitrogen atom. The remaining two resonance structures would have different double bond oxygen-nitrogen combinations.
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